NDC 53808-0686
Amlodipine 10 mg tablet
On the label: State of Florida DOH Central Pharmacy. It's repackaged from NDC 57664-570, which isn't on any FDA listing we can find.
Where the pills inside were made
This label doesn't name the factory that makes the drug (it lists 1 site that repackages it). Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants State of Florida DOH Central Pharmacy names for other drugs.
Product details
- Generic drug
- Amlodipine: every company that makes it
- Form
- tablet
- Strength
- 10 mg
- Approval
- ANDA ANDA078231
- On the market since
- Jan 1, 2013
- Package NDCs
53808-0686-1- Official label
- DailyMed (National Library of Medicine), updated Aug 9, 2013
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?